Canonical Allele Identifier: PA270587
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys317Arg
CA270586
NM_001110792.2:c.950A>G